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Article
Synthesis of 4,11-dideoxydaunomycinone by a Claisen/Diels-Alder sequence
The Journal of Organic Chemistry
  • George A. Kraus, Iowa State University
  • Spiors Liras, Iowa State University
  • Tim On Man, Iowa State University
  • Maria T. Molina, Instituto de Quimica Medica
Document Type
Article
Publication Version
Published Version
Publication Date
6-1-1989
DOI
10.1021/jo00274a033
Abstract

The synthesis of 3 from ketone 6 by a Claisen/Diels-Alder sequence uncovered some fascinating differences between the benzene and naphthalene series. The most direct pathway to 3 is 6-20-21-16-17-18.

Comments

Reprinted (adapted) with permission from The Journal of Organic Chemistry, 54(13); 3137-3139. Doi: 10.1021/jo00274a033. Copyright 1989 American Chemical Society.

Copyright Owner
American Chemical Society
Language
en
File Format
application/pdf
Citation Information
George A. Kraus, Spiors Liras, Tim On Man and Maria T. Molina. "Synthesis of 4,11-dideoxydaunomycinone by a Claisen/Diels-Alder sequence" The Journal of Organic Chemistry Vol. 54 Iss. 13 (1989) p. 3137 - 3139
Available at: http://works.bepress.com/george_kraus/101/